ClinVar Miner

List of variants in gene CREBBP reported as pathogenic for See cases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
GRCh37/hg19 16p13.3(chr16:3814227-3929941)x1
GRCh37/hg19 16p13.3(chr16:3922991-4004415)x1
GRCh38/hg38 16p13.3(chr16:3726714-3759009)x1
GRCh38/hg38 16p13.3(chr16:3750305-3769722)x3
GRCh38/hg38 16p13.3(chr16:3850966-3884581)x1
GRCh38/hg38 16p13.3(chr16:3861794-3904192)x1

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